510(k) K172253 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Altus Spine Cervical Interbody Fusion System
| Applicant | Altus Partners, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Nov 21, 2017 |
| Received | Jul 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172253
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.